CN1125843C - Method for preparing water-covered siloxane emulsion - Google Patents
Method for preparing water-covered siloxane emulsion Download PDFInfo
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- CN1125843C CN1125843C CN99115974A CN99115974A CN1125843C CN 1125843 C CN1125843 C CN 1125843C CN 99115974 A CN99115974 A CN 99115974A CN 99115974 A CN99115974 A CN 99115974A CN 1125843 C CN1125843 C CN 1125843C
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- A61K8/898—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing nitrogen, e.g. amodimethicone, trimethyl silyl amodimethicone or dimethicone propyl PG-betaine
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Abstract
A silicone oil-in-water emulsion containing a linear non-crosslinked silicone copolymer is prepared by polymerizing an OH endblocked polydiorganosiloxane with an amine functional trialkoxysilane in the presence of a metal catalyst. However, the polymerization is interrupted by the emulsification of this copolymer, and a carboxylic anhydride is added prior to the emulsification. The resulting emulsions are particularly useful in most personal care applications, and they also have value in textile fibre treatment, leather lubrication, fabric softening, as release agents, in water based coatings, for oil drag reduction, lubrication, and for the facilitation of cutting of cellulose materials.
Description
Technical field
The present invention relates to a kind of method for preparing emulsion, particularly a kind of preparation contains the method for the water-covered siloxane emulsion of linear non-crosslinked silicone copolymers.
Background technology
The commercial emulsion that contains a kind of amine-functionalized polydimethylsiloxane fluid, demand in market is restricted, this is because they only contain low viscous relatively amine-functionalized polydimethylsiloxane fluid, and they are for having the amine-functionalized polydimethylsiloxane of viscosity up to about 25000mm2/s in the time of 25 ℃.But the emulsion for the straight chain amine functionalized poly dimethyl silicone fluids that contains higher molecular weight and corresponding viscosity higher still exists demand, especially in the field of personal-care supplies.
And, in these commercial emulsions, except low viscous amine-functionalized polydimethylsiloxaneand fluid, also often may contain 1% the volatile X 2-1401 species of having an appointment, as octamethylcyclotetrasiloxane, the content of this volatile species is nonconforming according to recently safety and environmental regulations regulations.
Although the volatile cyclic species content is lower than 0.5% viscosity higher polysiloxane polymer, can react in the presence of catalyzer by some polysiloxane and linking agent and obtain, the prolongation of this class chain can adopt the end capped polydimethylsiloxane of a kind of OH and a kind of dialkoxy silicane to obtain already.This method is very slow, wants the time in several weeks just can finish usually.If attempt improves this method to add the carrying out of fast response, then adopt trialkoxy silane to substitute dialkoxy silicane, this will cause the formation of cross-linking elasticity material, and this material does not wish to exist in many application.
Prior art has been mentioned a kind of emulsion that contains amine-functionalized polydimethylsiloxane, but the particular viscosity or the molecular weight of the amine-functionalized polydimethylsiloxane fluid that these inventions are not all mentioned in the emulsion being contained, though or mentioned the viscosity or the molecular weight of amine-functionalized polydimethylsiloxane fluid, produce the level that reaches of requiring but be lower than present personal care articles for use field significantly.In some patent,, in these patents, all the preparation of this emulsion is kept silent usually although related to the amine-functionalized polydimethylsiloxaneand fluid of viscosity higher or higher molecular weight.US5326483 is exactly an example.
Though the applicant knows, there are many prior arts to riddle among the patent, they all relate to the dissimilar curing system that contains high viscosity and high-molecular weight polysiloxane, but, adopt trialkoxy silane so as body mutually in end capped polydiorganosiloxane of polymerization OH or polydimethylsiloxane, and thereby by this method, to prepare a kind of linear non-crosslinked siloxane polymer of high-molecular weight that is the emulsion form, this method is still unknown.
In addition, following method also is unknown, promptly carry out a kind of polyreaction, add a kind of acid anhydrides then and pass through emulsifying effect, thereby end the polyreaction process, particularly in the siloxane systems of end capped polydimethylsiloxane or polydiorganosiloxane based on OH, known it be unsettled and be easy to reverse, as the poly-effect of unzipping or back.However, by directly add a spot of a kind of carboxylic acid anhydride in siloxane polymer, the applicant has found that it is a kind of effective ways of avoiding this reverse before its emulsification.
Summary of the invention
The invention provides the method that a kind of preparation contains the water-covered siloxane emulsion of linear non-crosslinked silicone copolymers, it is characterized in that this method is made up of the following step successively: (A) in the presence of a kind of organotin catalysts, make the end capped polydiorganosiloxane of a kind of OH with in each component gross weight in polymerization procedure (A), greater than 0 but at the most a kind of amine-functionalized trialkoxy silane of 5 weight % carries out polymerization; (B) add a kind of carboxylic acid anhydride in the reaction product of step (A), the amount of this carboxylic acid anhydride is enough to polyreaction be slowed down and (C) then multipolymer prepared in polymerization procedure (A) is carried out emulsification.
The present invention can utilize a kind of siloxanes curing system of trialkoxy silane that wherein adopted to prepare siloxane polymer, and when the viscosity of expection had reached, the present invention can add and the emulsifying effect step by an acid anhydrides, and polyreaction is ended.Although this method can be used to prepare and contains the emulsion that range of viscosities is about 1000mm2/sec one 1000000mm2/sec siloxane polymer, most preferably the viscosity that has of the siloxane polymer in the emulsion usually its scope be about 30000mm2/sec-500000mm2/sec.
Like this,,, and when polymkeric substance also is in linearity, carry out a polyreaction aborting step, just can obtain linear siloxane polymer if adopt a spot of trialkoxy silane according to the present invention.Therefore, in fact, emulsifying effect is used for ending polyreaction.Passing through in polymkeric substance, to introduce a kind of acid anhydrides before the emulsification, can avoid the reverse of polymkeric substance.
In by the benefit that the present invention obtained, comprise and to obtain a kind of useful siloxane emulsion, it contains more high-molecular weight linear amines functional polysiloxane polymkeric substance, and it is than adopting the present polymkeric substance that technology of preparing obtained to have the hair conditioning performance of improvement.
In addition, compare with employing dialkoxy silicane technology, adopting trialkoxy silane can significantly be the kinetics speed of accelerating polyreaction, beat allly be, if adopt a spot of trialkoxy silane, it can not cause the generation of cross-linked material, and, also can polyreaction be ended by the interpolation and the emulsifying effect of acid anhydrides.Though the consumption of trialkoxy silane by weight can be high to about 5%, preferably its consumption normally is lower than about 3% by weight.
The method according to this invention mainly is to carry out two steps.First step comprises preferably polydimethylsiloxane of the end capped polydiorganosiloxane of OH, in the presence of a kind of metal catalyst, with the polyreaction of amine-functionalized trialkoxy silane.In second step, by adding a kind of acid anhydrides and, the condensation reaction of the carrying out in first step being ended by emulsifying effect as the result who adds one or more tensio-active agents and water.
Embodiment
Be used for the polydiorganosiloxane in the above-mentioned reaction of this method first step, generally include a kind of linear substantially polymkeric substance, its structure is:
In this structure, each R represents to have the alkyl that can reach 20 carbon atoms respectively, and as alkyl, representational example has methyl, ethyl, propyl group or butyl.Also a kind of aryl of R such as phenyl.R ' expression-OH, n are the positive integer greater than 1.Preferred n is an integer, makes the polysiloxane of polymkeric substance have viscosity at 25 ℃ and is about 1-1 * 106mm2/sec.
If necessary, this polydiorganosiloxane can have a spot of side chain, as is lower than the 2mole% of siloxane units, and can not influence the present invention, that is, this polymkeric substance is linear substantially.Preferably, all R groups all are methyl.
The organosilicon raw material that reacts with the end capped polydiorganosiloxane of OH in condensation reaction is a kind of amine-functionalized trialkoxy silane.This material useful molecules formula Q-Si-(OR ") 3 expressions, R wherein " for containing the alkyl of 1-6 carbon atom; Q represents the amine-functionalized substituting group of a kind of expression for-R Z, and R wherein is a kind of divalent alkyl with 3-6 carbon atom; Z is a univalent perssad, is selected from by-NR2 " " and-NR " " (CH2) mNR2 " " group formed, R wherein " " expression hydrogen or a kind of alkyl with 1-4 carbon, the value of m is the positive integer of 2-6.
Suitable R " group is selected from methyl, ethyl, propyl group, sec.-propyl, butyl and isobutyl-respectively.
The alkylidene group of representing with R can comprise trimethylene, tetramethylene, pentamethylene ,-CH
2CHCH
3CH
2-and-CH
2CH
2CHCH
3CH
2-.R wherein is the trimethylene that replaces of trimethylene or a kind of alkyl as-CH
2CHCH
3CH
2-silane be preferred.
Useful Z group comprises unsubstituted amino-NH2, and the amino that alkyl replaces is as-NHCH
3,-NHCH
2CH
2CH
2CH
3With-N (CH
2CH
3)
2The amino that replaces with aminoalkyl group is as-NHCH
2CH
2NH
2,-NH (CH
2)
6NH
2With-NHCH
2CH
2N (CH
3)
2
The part representative example of the amine-functionalized trialkoxy silane that the commerce that can adopt can get has: the amino butyl triethoxyl silane of 4-; N-(2-amino-ethyl)-3-TSL 8330; N-(the amino hexyl of 6-) aminopropyl trimethoxy silane; 3-aminopropyl triethoxy alkyl; The 3-TSL 8330; (3-aminopropyl) three [2-(2-methoxy ethoxy) oxyethyl group] silane; And 3-[2-(the amino ethylamino of 2-) ethylamino] propyl group-Trimethoxy silane.
If necessary, the three functionalized alcoxyl silane of other type also can be used for this place, the trialkoxy silane of epoxy functional for example, the trialkoxy silane that trialkoxy silane that acryloxy is functionalized and methacryloxy are functionalized.The representative example that can adopt comprises: 3-(Racemic glycidol oxygen propyl group) Trimethoxy silane, [β-(3, the 4-epoxycyclohexyl) ethyl] Trimethoxy silane, 5,6-(epoxy group(ing) hexyl) Trimethoxy silane, 3-(acryloxy propyl group) Trimethoxy silane, and 3-(methacryloxypropyl) Trimethoxy silane.
The metal catalyst that is used for ≡ Si-OH and ≡ Si-OR reaction is preferably a kind of organic tin salt, and the part example comprises stannous octoate, two lauric acid tin methides, dibutyl tin laurate, dibutyltin diacetate, two neodecanoic acid tin methides, dimethoxy dibutyl tin, glycerine three cerinic acid isobutyl-tin, two butyric acid tin methides, tartrate triethyltin, oleic acid tin, naphthenic acid tin, butyric acid tin, tin acetate, phenylformic acid tin, sebacic acid tin and succsinic acid tin.Usually, catalyst consumption is about the 0.001-10% of the end capped polydiorganosiloxane weight of OH.
The polyreaction of carrying out in the first step of present method is a condensation reaction, and it includes the end capped polydiorganosiloxane of OH, amino-trialkoxy silane and metal catalyst, and it can obtain explanation by the particular instance that describes below.
This condensation reaction can make it to slow down by adding a kind of acid anhydrides, preferably adds a kind of carboxylic acid anhydride, as diacetyl oxide (CH
3CO)
2O or benzoyl oxide (C
6H
5CO)
2O.Other carboxylic acid anhydride also can adopt, as succinyl oxide, Tetra hydro Phthalic anhydride and maleic anhydride.
After this adds step, adopt water and a kind of suitable tensio-active agent or surfactant mixtures, make the end capped amine-functionalized silicone copolymers generation emulsification of resulting linear OH.
Described tensio-active agent can be nonionogenic tenside, cats product, anion surfactant, alkyl polysaccharide class or amphoterics.
The example of nonionogenic tenside comprises polyoxyalkylene alkyl ether, polyoxy alkylidene sorbitanic alkyl ester, polyoxy alkylidene alkyl ester and polyoxy alkylidene alkyl phenol ether, poly-ethylidene binary alcohol, polytrimethylene dibasic alcohol and diethylidene dibasic alcohol.
The example of cats product comprises: the oxyhydroxide of quaternary ammonium salt such as tetramethyl ammonium hydroxide, methylsulfuric acid hexadecyl trimethyl ammonium, acetate alkyl trihydroxy-ethyl ammonium, hydroxide octyl group trimethyl ammonium, hydroxide dodecyl trimethyl ammonium, cetyltrimethylammonium hydroxide trimethyl ammonium, hydroxide octyldimethyl phenyl ammonium, hydroxide decyl 3,5-dimethylphenyl ammonium, hydroxide two (dodecyl) Dimethyl Ammonium, hydroxide two (octadecyl) Dimethyl Ammonium, hydroxide tallow trimethyl ammonium, hydroxide cocounut oil trimethyl ammonium, and its corresponding salt of these materials; Fatty acid amine and acid amides and their derivative, and the salt of fatty acid amine and acid amides, comprise aliphatic aliphatic amide and their derivative, have the arylamine thing of the same clan of aliphatic chain, the aliphatic acid amides that comes from aliphatic diamine, the derivative that comes from dibasic amine deutero-aliphatic series acid amides, quadrol, the amide derivatives of alkamine, the amine salt of longer chain fatty acid, the quaternary ammonium hydroxide that comes from the aliphatic acid amides of two replacement diamines, the quaternary ammonium hydroxide of benzimidazoline; The basic cpd of pyridinium salt and derivative thereof; The compound of sulfonium; The quaternary ammonium compound of trimethyl-glycine; The urethane of quadrol; Polyethyene diamine; With the poly-thanomin of poly-propyl alcohol.
Suitable anion surfactant example comprises: alkyl sodium sulfate ester such as sulfuric acid dodecyl ester; Polymkeric substance such as acrylate/C
10-30Alkyl acrylate cross-linked polymer; Alkyl benzene sulphonate (ABS) and salt thereof are as hexyl benzene sulfonic acid, octyl group Phenylsulfonic acid, decyl Phenylsulfonic acid, dodecyl Phenylsulfonic acid, hexadecyl Phenylsulfonic acid and nutmeg base Phenylsulfonic acid; The sulfuric ester of monoalkyl polyoxyethylene ether; Alkyl naphthalene sulfonic acid; The basic metal sulforicinate; The sulfonated glycerin fatty acid ester is as condensation product, the octahydro anthracene sulfonic acid sodium of sulfonated products, sulfonated aryl hydrocarbon, naphthene sulfonic acid and the formaldehyde of the salt of sulfonated cocinic acid direactive glyceride, sulfonated monovalence alcohol ester, sulfamic acid amides, fatty acid nitrile; Alkali metal alkyl sulfate; Sulfuric ester; And alkyl aryl sulfonate.
The alkyl polysaccharide class tensio-active agent example that part is suitable comprises: for example, structural formula is R
1-O-(R
2O) material of a (G) b, R wherein
1The thiazolinyl or the alkyl phenyl of alkyl, linearity or the side chain of expression linearity or side chain; R
2The expression alkylidene group; G is a kind of as-reduced sugar; A represents 0 or positive integer; B represents a positive integer.The tensio-active agent of these types described in detail already, for example in US5035832.
Suitable examples of amphoteric surfactants comprises cocamidopropyl betaine and cocamidopropyl propyl hydroxy sulfuric ester.
Above-mentioned tensio-active agent can use separately, also can unite use.
The particle size of the siloxanes in the emulsion except other factors, also depends on the consumption and the kind of the tensio-active agent that is adopted.The consumption of tensio-active agent changes with tensio-active agent, but usually, its consumption is about the 1-30% of the end capped polydiorganosiloxane gross weight of OH.Particle size range is initiated with 0.2 μ m, but is preferably about 0.3 μ m to 1.5 μ m.
The material that is used for forming emulsion at last is a water, and it can form the external phase of emulsion, and the silicone oil droplet can be distributed to wherein and go.
If necessary, other material also can join among arbitrary phase of emulsion.For example, can comprise perfume, tinting material, thickening material, sanitas, plasticizer and activeconstituents such as medicine.
Preferable methods is that linear OH end capped amine-functionalized silicone copolymers, tensio-active agent and hydromining are mixed with easy alr mode, forms a kind of thick water-in-oil mixture.This mixture then carries out emulsification.In the emulsifying effect process, described thick water-in-oil mixture is converted into a kind of thin silicon water-covered siloxane emulsion.This emulsifying effect can adopt traditional device such as batch mixer, colloidal mill or straight line mixture (line mixer).Therefore, this emulsification method is simple and efficient.
The end capped amine-functionalized silicone copolymers of linear OH, tensio-active agent and water can disposablely mix, and these materials also can mix in any order, as long as water is just passable as last component.
Emulsion of the present invention is useful in the occasion of many standard application siloxane emulsions.Therefore, they are applicable to the Application Areas of personal care.As be used for hair, skin, mucus and tooth.In these are used, siloxanes is slick, it can improve the performance of following material, protective skin cream, skin cream, moistening agent, facial treatment agent such as acne remover or the agent of going to wrinkle, individual and facial cleansing agent, bathe oil, perfume, spices, cologne, face powder, sun-screening agent, in advance shave liquid and after shave liquid, shaving soap and shaving foam.Similarly, it also can be used for shampoo, hair conditioner, hair jelly, mousse, permanent wave solution, alopecia agent and cuticula coating, can be used to provide conditioning effect preferably.In makeup, it is homogenizing and spreading agent as pigment, is used for cosmetics, additive color makeup, end powder, kermes, lipstick, eyeliner, mascara, degreaser, additive color makeup remover and cosmetics.Similarly, it also can be used as the delivery system of the material of a kind of oil and water soluble, as VITAMIN, organic sunscreen agent, ceramide and medicine.When being combined into to spillikin, gel, washing lotion, aerosol and ball, emulsion of the present invention has increased a compensating action that drying is soft and smooth.
When being used for personal-care supplies, the add-on of emulsion is generally about 0.01-50% of personal-care supplies weight, preferably is about 0.1-25%.They can add among traditional composition that is used for personal-care supplies.Therefore, they can mix mutually with the component of deposited polymer, tensio-active agent, washing composition, antiseptic-germicide, antidandruff agent, whipping agent, protein, moistening agent, suspension agent, opalizer, perfume, tinting material, plant extraction liquid, polymkeric substance and other traditional personal-care supplies.
Except personal-care supplies, emulsion of the present invention also can be used for other application, the summary of the plain material of drag reduction, lubricating oil and cutting fibre of, releasing agent softening as textile fibres processing, harness oil, fabric, water-based paint, oil.
Described here not away from mixture, composition and the method for principal character of the present invention, other variation also can be arranged.
Example given below will be described in more detail the present invention.Except as otherwise noted, all components and per-cent all are by weight, and viscosity is measured down at 25 ℃.Example 1
Preparing a kind of cationic emulsion, is to be about 560 the end capped polydimethylsiloxane of OH, the tin catalyst of 0.1g and N-(2-amino-ethyl)-3-TSL 8330 of 0.26g by the polymerization degree of mixing 49.64g to prepare.Used in this example tin catalyst is two neodecanoic acid tin methides.The meaning of the polymerization degree is about 560 for the numerical value of " n " in the monomeric molecular formula of aforesaid expression polydimethylsiloxane.Therefore, this polydimethylsiloxane monomer has the (CH with molecular formula HO
3)
2SiO[(CH
3)
2SiO]
560Si (CH
3)
2The OH corresponding structure.Obtaining a kind of viscosity at 40 ℃ in following 35 minutes is 100000mm
2The siloxane polymer that/s is amine-functionalized.It is flowable, and can be used for machinery emulsification.In order to stop further polyreaction, then carry out inversion phase emulsion.It is to realize by the diacetyl oxide that adds 0.4g in polymkeric substance, thereby has avoided any reverse depolymerization reaction.Afterwards, the Arquad 16-29 and the 4g water that add Renex 30, the 2g of 3g again.What need more explanation is that Arquad16-29 is a kind of cats product and a kind of chlorination N-alkyl trimethyl ammonium.It is AkzoChemicals, Inc., Chicago, the product of Illinois.Renex 30 is that a kind of HLB is 14.5 nonionogenic tenside.It is a kind of polyoxyethylene ether alcohol, is ICI Surfactants, Wilmington, the product that Delaware produces.
Mixture is sheared fully,, proceeded shearing action, be reduced within about 0.3-0.8 micrometer range until obtaining particle size to realize inversion of phases.The dilution water that in through the mixture of shearing, adds 40.6g.
And Research on The Rheology emulsifying polymers prepared to this example shows, crosslinked action does not take place.This can be confirmed by tan delta or loss factor, and it is coefficient of viscosity G " with the ratio of coefficient of elasticity G ', be 100000mm corresponding to the known viscosity of tan deltas
2The linear amines functionalized silicone polymkeric substance of/s, the numerical value that it has usually is about 10 when 1 hertz (Hz).It is pointed out that tan delta be a kind of usually about and be used for characterizing cross-linked material such as elastomeric character, its method of calculation and meaning have detailed explanation in US5449560.
In order to guarantee that the polymer droplets in the emulsion no longer continues further to carry out polyreaction, can adopt classical methyl alcohol/hexane demulsification technology that polymkeric substance is extracted from emulsion, and measure its viscosity.The viscosity of finding its viscosity and emulsifying effect straight polymer before is consistent.It is carried out gas-chromatography (GC) analysis, and to determine whether to exist volatile cyclosiloxane, they may form as by product in preparation process, as species octamethylcyclotetrasiloxane (D4).Analytical results shows and only contains 0.1% the D4 of having an appointment.Example 2-4
Repeat example 1, the consumption that different is is used for the tin catalyst of these three examples is 0.2%.The consumption that is used for N-(2-the amino-ethyl)-3-TSL 8330 of these three examples also is different, visible following table 1.Example 2 has the different polymerization degree (DP) with the 3 end capped polydimethylsiloxanes of OH that adopt, and its DP can see Table 1.On the other hand, example 4 is adopted is that its polymerization degree of containing weight ratio 80% is about 560 the end capped polydimethylsiloxane of OH and its viscosity of 20% is 90mm
2The mixture of the end capped polydimethylsiloxane of OH of/s.
Table 1
Example 5-7
| The PDMS DP472 that example 2 is short | The PDMS DP945 that example 3 is long | The mixing of 42 kinds of PDMS of example (DP 560/DP 100) | |
| The amount of aminosilane | 0.64％ | 0.33％ | 3％ |
| Reach 100000mm 2The time of/s | 340 minutes | 38 minutes | 550 minutes |
| Tan Delta when 1Hz | 8.8 | 10.4 | 2.7 |
Adopt the end capped PDMS of identical OH to repeat example 1, but the consumption of used N-(2-amino-ethyl)-3-TSL 8330 is 0.52% by weight.Through the resulting result of inversion phase emulsion is 100000mm
2The amine-functionalized siloxanes of/s.The kind that is used for the tensio-active agent of emulsifying effect in these three examples also is different with example 1, visible following table 2.More explanation is, Elfan NS-242 is a kind of alkyl sodium sulfate ester of ethoxylation, can be by Akzo Chemicals BV, and Amersfoort, TheNetherlands obtains.
Table 2
Example 8-10
| Example 5 cats products | Example 6 nonionogenic tensides | Example 7 anion surfactants | |
| Title and consumption | ARQUAD 16-29 5％ | RENEX 30 4％ | ELFAN NS-242 4％ |
| Transform water consumption | 0％ | 4％ | 15％ |
| Particle size | 1.5μm | 0.4μm | 1μm |
Adopt identical raw material to repeat example 1.The consumption of used tin catalyst is 0.2% by weight.The visible following table 3 of consumption that is used for N-(2-the aminoethyl)-3-TSL 8330 of these three examples.It is 100000mm to viscosity that these examples have provided the silane consumption
2The influence of the crosslinking degree of/s multipolymer (by Tan Delta materialization).
Table 3
Example 11
| The aminosilane of example 8 0.44% | The aminosilane of example 9 0.52% | The aminosilane of example 10 0.62% | |
| Arrive 100000mm 2The time of/s | 450 minutes | 134 minutes | 82 minutes |
| Tan Delta when 1Hz | 11.8 | 9.9 | 3.7 |
In this example, a kind of known amine-functionalized silicone resin through depolymerization compares being used for as standard.Its viscosity is about 85000mm
2/ s is about 10.7 at the tan at 1Hz place delta.Adopt method of the present invention to prepare the amine-functionalized siloxanes that a kind of viscosity is the equivalence of 85000mm2/s.Its tandelta is about 13.This functionalized siloxanes that is subjected to that shows that the present invention prepares has better plastic performance, thereby has more weak elasticity.This just proves and wherein has the very branched monomer of low number, proves that method of the present invention can be used to the polymkeric substance of production of linear.
Claims (11)
1. method for preparing the water-covered siloxane emulsion that contains linear non-crosslinked silicone copolymers, it is characterized in that this method is made up of the following step successively: (A) in the presence of a kind of organotin catalysts, make the end capped polydiorganosiloxane of a kind of OH with in each component gross weight in polymerization procedure (A), greater than 0 but at the most a kind of amine-functionalized trialkoxy silane of 5 weight % carries out polymerization; (B) add a kind of carboxylic acid anhydride in the reaction product of step (A), the amount of this carboxylic acid anhydride is enough to polyreaction be slowed down and (C) then multipolymer prepared in polymerization procedure (A) is carried out emulsification.
2. method according to claim 1 is characterized in that described carboxylic acid anhydride is to be selected from the group of being made up of diacetyl oxide, benzoyl oxide, succinyl oxide, Tetra hydro Phthalic anhydride and maleic anhydride.
3. the described method of claim 1 is characterized in that the end capped polydiorganosiloxane of described OH comprises a kind of polymkeric substance of linearity, and its structure is:
Wherein, each R represents to have the alkyl or the aryl of 1-20 carbon atom respectively; R ' represents OH; N is the positive integer greater than 1.
4. the described method of claim 1 is characterized in that described amine-functionalized trialkoxy silane monomer is to be selected from the amino butyl triethoxyl silane by 4-;
N-(2-amino-ethyl)-3-TSL 8330;
N-(the amino hexyl of 6-) aminopropyl trimethoxy silane;
3-aminopropyl triethoxy alkyl; The 3-TSL 8330;
(3-aminopropyl) three [2-(2-methoxy ethoxy) oxyethyl group] silane; With
3-[2-(2-amino ethylamino) ethylamino] group formed of propyl group-Trimethoxy silane.
5. the described method of claim 1 is characterized in that described organotin catalysts is to be selected from the group of being made up of stannous octoate, two lauric acid tin methides, dibutyl tin laurate, dibutyltin diacetate, two neodecanoic acid tin methides, dimethoxy dibutyl tin, glycerine three cerinic acid isobutyl-tin, two butyric acid tin methides, tartrate triethyltin, oleic acid tin, naphthenic acid tin, butyric acid tin, tin acetate, phenylformic acid tin, sebacic acid tin and succsinic acid tin.
6. each described method of aforementioned claim is characterized in that described multipolymer is to adopt a kind of nonionogenic tenside to carry out emulsive.
7. each described method of claim 1-5 is characterized in that described multipolymer is to adopt nonionogenic tenside and ionic surface active agent to unite to carry out emulsive.
8. each described method of claim 1-5 is characterized in that described multipolymer is to adopt a kind of cats product to carry out emulsive.
9. each described method of claim 1-5 is characterized in that described multipolymer is to adopt a kind of anion surfactant to carry out emulsive.
10. each described method of claim 1-5, it is characterized in that described silicone copolymers at 25 ℃ of its range of viscosities at 30000mm
2/ s-500000mm
2Between/the s, the average particle size particle size scope of described emulsion is between 0.3 micron-1.5 microns.
11. the described method of claim 4, the amine-functionalized trialkoxy silane that it is characterized in that being adopted is to be lower than each component gross weight in polymerization procedure (A), greater than 0 but less than 3 weight %.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9826394.0 | 1998-12-02 | ||
| GBGB9826394.0A GB9826394D0 (en) | 1998-12-02 | 1998-12-02 | Method of making silicone-in-water emulsions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1260358A CN1260358A (en) | 2000-07-19 |
| CN1125843C true CN1125843C (en) | 2003-10-29 |
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ID=10843447
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN99115974A Expired - Lifetime CN1125843C (en) | 1998-12-02 | 1999-12-02 | Method for preparing water-covered siloxane emulsion |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6248855B1 (en) |
| EP (1) | EP1013700B1 (en) |
| JP (1) | JP4611477B2 (en) |
| KR (1) | KR100677173B1 (en) |
| CN (1) | CN1125843C (en) |
| AT (1) | ATE224418T1 (en) |
| AU (1) | AU6300899A (en) |
| DE (1) | DE69902988T2 (en) |
| GB (1) | GB9826394D0 (en) |
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|---|---|---|---|---|
| CN111032786A (en) * | 2017-07-24 | 2020-04-17 | 陶氏东丽株式会社 | Oil-in-water emulsion composition, method for producing same, and use thereof |
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| GB0302840D0 (en) * | 2003-02-07 | 2003-03-12 | Dow Corning | Process for making silicone emulsions |
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-
1998
- 1998-12-02 GB GBGB9826394.0A patent/GB9826394D0/en not_active Ceased
-
1999
- 1999-12-01 AU AU63008/99A patent/AU6300899A/en not_active Abandoned
- 1999-12-01 EP EP99309662A patent/EP1013700B1/en not_active Expired - Lifetime
- 1999-12-01 DE DE69902988T patent/DE69902988T2/en not_active Expired - Lifetime
- 1999-12-01 AT AT99309662T patent/ATE224418T1/en not_active IP Right Cessation
- 1999-12-02 KR KR1019990054412A patent/KR100677173B1/en active IP Right Grant
- 1999-12-02 JP JP34359999A patent/JP4611477B2/en not_active Expired - Lifetime
- 1999-12-02 US US09/453,142 patent/US6248855B1/en not_active Expired - Lifetime
- 1999-12-02 CN CN99115974A patent/CN1125843C/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111032786A (en) * | 2017-07-24 | 2020-04-17 | 陶氏东丽株式会社 | Oil-in-water emulsion composition, method for producing same, and use thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1260358A (en) | 2000-07-19 |
| GB9826394D0 (en) | 1999-01-27 |
| JP4611477B2 (en) | 2011-01-12 |
| EP1013700B1 (en) | 2002-09-18 |
| KR100677173B1 (en) | 2007-02-02 |
| DE69902988T2 (en) | 2003-05-28 |
| ATE224418T1 (en) | 2002-10-15 |
| JP2000198852A (en) | 2000-07-18 |
| KR20000047856A (en) | 2000-07-25 |
| AU6300899A (en) | 2000-06-08 |
| EP1013700A3 (en) | 2001-04-11 |
| DE69902988D1 (en) | 2002-10-24 |
| US6248855B1 (en) | 2001-06-19 |
| EP1013700A2 (en) | 2000-06-28 |
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